CA3229752A1 - Derives nucleosidiques et leurs promedicaments ayant une action inhibitrice de la croissance virale - Google Patents
Derives nucleosidiques et leurs promedicaments ayant une action inhibitrice de la croissance virale Download PDFInfo
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- CA3229752A1 CA3229752A1 CA3229752A CA3229752A CA3229752A1 CA 3229752 A1 CA3229752 A1 CA 3229752A1 CA 3229752 A CA3229752 A CA 3229752A CA 3229752 A CA3229752 A CA 3229752A CA 3229752 A1 CA3229752 A1 CA 3229752A1
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- substituent group
- hydrogen
- optionally substituted
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- alkyl
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- 231100000211 teratogenicity Toxicity 0.000 description 1
- 125000000037 tert-butyldiphenylsilyl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1[Si]([H])([*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 125000005063 tetradecenyl group Chemical group C(=CCCCCCCCCCCCC)* 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 description 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 1
- 125000005942 tetrahydropyridyl group Chemical group 0.000 description 1
- ISXOBTBCNRIIQO-UHFFFAOYSA-N tetrahydrothiophene 1-oxide Chemical compound O=S1CCCC1 ISXOBTBCNRIIQO-UHFFFAOYSA-N 0.000 description 1
- 125000003831 tetrazolyl group Chemical group 0.000 description 1
- 125000001113 thiadiazolyl group Chemical group 0.000 description 1
- 125000005458 thianyl group Chemical group 0.000 description 1
- 125000004305 thiazinyl group Chemical group S1NC(=CC=C1)* 0.000 description 1
- 125000001984 thiazolidinyl group Chemical group 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 125000001730 thiiranyl group Chemical group 0.000 description 1
- 125000001166 thiolanyl group Chemical group 0.000 description 1
- 125000005505 thiomorpholino group Chemical group 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229940098465 tincture Drugs 0.000 description 1
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 238000013519 translation Methods 0.000 description 1
- 230000014616 translation Effects 0.000 description 1
- 125000004306 triazinyl group Chemical group 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- 125000005040 tridecenyl group Chemical group C(=CCCCCCCCCCCC)* 0.000 description 1
- UYPYRKYUKCHHIB-UHFFFAOYSA-N trimethylamine N-oxide Chemical compound C[N+](C)(C)[O-] UYPYRKYUKCHHIB-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- FTVLMFQEYACZNP-UHFFFAOYSA-N trimethylsilyl trifluoromethanesulfonate Chemical compound C[Si](C)(C)OS(=O)(=O)C(F)(F)F FTVLMFQEYACZNP-UHFFFAOYSA-N 0.000 description 1
- CWMFRHBXRUITQE-UHFFFAOYSA-N trimethylsilylacetylene Chemical group C[Si](C)(C)C#C CWMFRHBXRUITQE-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- HDYANYHVCAPMJV-USQUEEHTSA-N udp-glucuronic acid Chemical compound O([P@](O)(=O)O[P@](O)(=O)OC[C@H]1[C@@H]([C@H]([C@@H](O1)N1C(NC(=O)C=C1)=O)O)O)[C@H]1O[C@@H](C(O)=O)[C@H](O)[C@@H](O)[C@@H]1O HDYANYHVCAPMJV-USQUEEHTSA-N 0.000 description 1
- 125000005065 undecenyl group Chemical group C(=CCCCCCCCCC)* 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 230000005727 virus proliferation Effects 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 125000001834 xanthenyl group Chemical group C1=CC=CC=2OC3=CC=CC=C3C(C12)* 0.000 description 1
- 229940051021 yellow-fever virus Drugs 0.000 description 1
- 210000001325 yolk sac Anatomy 0.000 description 1
- GTLDTDOJJJZVBW-UHFFFAOYSA-N zinc cyanide Chemical compound [Zn+2].N#[C-].N#[C-] GTLDTDOJJJZVBW-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/16—Antivirals for RNA viruses for influenza or rhinoviruses
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Virology (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Communicable Diseases (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Epidemiology (AREA)
- Molecular Biology (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
Abstract
La présente invention concerne un composé représenté par la formule (I). (Dans la formule, A est une base, etc ; R1 représente l'hydrogène, etc. ; R2 représente l'hydrogène, etc. ; R3 représente l'hydrogène, etc. ; R4a représente l'hydrogène, etc. ; R4b représente l'hydrogène, etc ; R5 représente l'hydrogène, etc ; et R6 représente l'hydrogène, etc.)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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JP2021134801 | 2021-08-20 | ||
JP2021-134801 | 2021-08-20 | ||
PCT/JP2022/031308 WO2023022216A1 (fr) | 2021-08-20 | 2022-08-19 | Dérivés nucléosidiques et leurs promédicaments ayant une action inhibitrice de la croissance virale |
Publications (1)
Publication Number | Publication Date |
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CA3229752A1 true CA3229752A1 (fr) | 2023-02-23 |
Family
ID=85240607
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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CA3229752A Pending CA3229752A1 (fr) | 2021-08-20 | 2022-08-19 | Derives nucleosidiques et leurs promedicaments ayant une action inhibitrice de la croissance virale |
Country Status (8)
Country | Link |
---|---|
JP (1) | JPWO2023022216A1 (fr) |
KR (1) | KR20240050362A (fr) |
AU (1) | AU2022331233A1 (fr) |
CA (1) | CA3229752A1 (fr) |
CO (1) | CO2024003018A2 (fr) |
IL (1) | IL310854A (fr) |
PE (1) | PE20240654A1 (fr) |
WO (1) | WO2023022216A1 (fr) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
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TW202228722A (zh) | 2020-08-27 | 2022-08-01 | 美商基利科學股份有限公司 | 用於治療病毒感染之化合物及方法 |
TWI811812B (zh) | 2020-10-16 | 2023-08-11 | 美商基利科學股份有限公司 | 磷脂化合物及其用途 |
TW202400185A (zh) | 2022-03-02 | 2024-01-01 | 美商基利科學股份有限公司 | 用於治療病毒感染的化合物及方法 |
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DE3277623D1 (en) | 1981-07-31 | 1987-12-17 | Sloan Kettering Inst Cancer | Anti-leukemic beta-glycosyl c-nucleosides |
US5985848A (en) | 1997-10-14 | 1999-11-16 | Albert Einstein College Of Medicine Of Yeshiva University | Inhibitors of nucleoside metabolism |
WO2002018371A1 (fr) | 2000-08-29 | 2002-03-07 | Industrial Research Limited | Inhibiteurs du metabolisme des nucleosides |
US7098334B2 (en) | 2002-03-25 | 2006-08-29 | Industrial Research Limited | 4-amino-5H-pyrrolo[3,2-d]pyrimidine inhibitors of nucleoside phosphorylases and nucleosidases |
CN1653077A (zh) | 2002-05-06 | 2005-08-10 | 健亚生物科技公司 | 治疗c型肝炎病毒感染的核苷衍生物 |
DK1628685T3 (da) | 2003-04-25 | 2011-03-21 | Gilead Sciences Inc | Antivirale phosphonatanaloge |
AU2005254057B2 (en) | 2004-06-15 | 2011-02-17 | Isis Pharmaceuticals, Inc. | C-purine nucleoside analogs as inhibitors of RNA-dependent RNA viral polymerase |
WO2006002231A1 (fr) | 2004-06-22 | 2006-01-05 | Biocryst Pharmaceuticals, Inc. | Azanucleosides, leur preparation et leur utilisation comme inhibiteur des arn polymerases virales |
KR20070100237A (ko) | 2004-10-29 | 2007-10-10 | 바이오크리스트 파마수티컬즈, 인코퍼레이티드 | 치료용 푸로피리미딘 및 티에노피리미딘 |
WO2007069924A1 (fr) | 2005-12-15 | 2007-06-21 | Industrial Research Limited | Analogues de déazapurine de 4'-aza-l-nucléosides |
SG177974A1 (en) | 2007-01-12 | 2012-02-28 | Biocryst Pharm Inc | Antiviral nucleoside analogs |
DK2155758T3 (da) | 2007-05-10 | 2012-11-05 | Biocryst Pharm Inc | Tetrahydrofuro[3,4-d]dioxolanforbindelser til anvendelse i behandlingen af virusinfektioner og cancer |
EP2313102A2 (fr) | 2008-07-03 | 2011-04-27 | Biota Scientific Management | Nucléosides bicycliques et nucléotides convenant comme agents thérapeutiques |
TW201305185A (zh) | 2010-09-13 | 2013-02-01 | Gilead Sciences Inc | 用於抗病毒治療之2’-氟取代之碳-核苷類似物 |
WO2012074912A1 (fr) | 2010-11-29 | 2012-06-07 | Albert Einstein College Of Medicine Of Yeshiva University | Procédés, essais et composés pour le traitement d'infections bactériennes par l'inhibition de la méthylthioinosine phosphorylase |
US9481704B2 (en) * | 2012-03-13 | 2016-11-01 | Gilead Sciences, Inc. | 2′-substituted carba-nucleoside analogs for antiviral treatment |
AR090699A1 (es) | 2012-04-18 | 2014-12-03 | Biocryst Pharm Inc | Compuestos inhibidores de la actividad de la arn polimerasa viral |
WO2014035140A2 (fr) | 2012-08-30 | 2014-03-06 | Kainos Medicine, Inc. | Composés et compositions pour la modulation de l'activité histone méthyltransférase |
US20150291596A1 (en) * | 2012-11-16 | 2015-10-15 | Biocryst Pharmaceuticals, Inc. | Antiviral azasugar-containing nucleosides |
EP2931319B1 (fr) | 2012-12-13 | 2019-08-21 | ModernaTX, Inc. | Molécules d'acide nucléique modifiées et leurs utilisations |
JP6417568B2 (ja) | 2013-05-14 | 2018-11-07 | バイオクリスト ファーマスーティカルズ,インコーポレイテッドBiocryst Pharmaceuticals,Inc. | 抗インフルエンザ組成物及び方法 |
UA119050C2 (uk) | 2013-11-11 | 2019-04-25 | Ґілеад Саєнсиз, Інк. | ПІРОЛО[1.2-f][1.2.4]ТРИАЗИНИ, ЯКІ ВИКОРИСТОВУЮТЬСЯ ДЛЯ ЛІКУВАННЯ РЕСПІРАТОРНО-СИНЦИТІАЛЬНИХ ВІРУСНИХ ІНФЕКЦІЙ |
WO2015143712A1 (fr) | 2014-03-28 | 2015-10-01 | Merck Sharp & Dohme Corp. | Inhibiteurs nucléosidiques substitués en 4' de la transcriptase inverse |
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WO2018230479A1 (fr) | 2017-06-13 | 2018-12-20 | 大原薬品工業株式会社 | Dérivé d'éther de silyle en position 5' pour agent anticancéreux nucléosidique ou agent anti-viral |
MA50172A (fr) * | 2017-09-18 | 2021-04-07 | Janssen Biopharma Inc | Nucléosides substitués, nucléotides et analogues de ceux-ci |
CA3126348A1 (fr) | 2018-01-12 | 2020-07-18 | Board Of Regents Of The University Of Nebraska | Promedicaments antiviraux et formulations de ceux-ci |
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CN112062800B (zh) | 2020-09-02 | 2022-11-18 | 广东东阳光药业有限公司 | 核苷化合物的氨基磷酸酯衍生物及其用途 |
CN112010916B (zh) | 2020-09-09 | 2022-12-27 | 广东东阳光药业有限公司 | 核苷化合物的氨基磷酸酯衍生物及其用途 |
-
2022
- 2022-08-19 AU AU2022331233A patent/AU2022331233A1/en active Pending
- 2022-08-19 CA CA3229752A patent/CA3229752A1/fr active Pending
- 2022-08-19 JP JP2023542451A patent/JPWO2023022216A1/ja active Pending
- 2022-08-19 PE PE2024000272A patent/PE20240654A1/es unknown
- 2022-08-19 IL IL310854A patent/IL310854A/en unknown
- 2022-08-19 KR KR1020247008024A patent/KR20240050362A/ko unknown
- 2022-08-19 WO PCT/JP2022/031308 patent/WO2023022216A1/fr active Application Filing
-
2024
- 2024-03-13 CO CONC2024/0003018A patent/CO2024003018A2/es unknown
Also Published As
Publication number | Publication date |
---|---|
AU2022331233A1 (en) | 2024-02-29 |
CO2024003018A2 (es) | 2024-03-18 |
JPWO2023022216A1 (fr) | 2023-02-23 |
WO2023022216A1 (fr) | 2023-02-23 |
IL310854A (en) | 2024-04-01 |
PE20240654A1 (es) | 2024-04-04 |
KR20240050362A (ko) | 2024-04-18 |
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